Precise quantification of cellular uptake of cell-penetrating peptides using fluorescence-activated cell sorting and fluorescence correlation spectroscopy

被引:52
作者
Rezgui, Rachid [1 ]
Blumer, Katy [2 ]
Yeoh-Tan, Gilbert [3 ]
Trexler, Adam J. [4 ]
Magzoub, Mazin [1 ]
机构
[1] New York Univ, Biol Program, POB 129188,Saadiyat Isl Campus, Abu Dhabi, U Arab Emirates
[2] New York Univ, Phys Program, Abu Dhabi, U Arab Emirates
[3] New York Univ, CGSB, Abu Dhabi, U Arab Emirates
[4] NHLBI, Lab Mol Biophys, NIH, Bldg 10, Bethesda, MD 20892 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2016年 / 1858卷 / 07期
基金
美国国家卫生研究院;
关键词
Drug delivery; Cellular uptake; Internalization pathways; Intracellular distribution; Intracellular degradation; Toxicity threshold; ARGININE-RICH PEPTIDES; CARGO MOLECULES; MEMBRANE; INTERNALIZATION; PROTEINS; DELIVERY; PLASMA; TRANSLOCATION; ENDOCYTOSIS; MECHANISM;
D O I
10.1016/j.bbamem.2016.03.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell-penetrating peptides (CPPs) have emerged as a potentially powerful tool for drug delivery due to their ability to efficiently transport a whole host of biologically active cargoes into cells. Although concerted efforts have shed some light on the cellular internalization pathways of CPPs, quantification of CPP uptake has proved problematic. Here we describe an experimental approach that combines two powerful biophysical techniques, fluorescence activated cell sorting (FACS) and fluorescence correlation spectroscopy (FCS), to directly, accurately and precisely measure the cellular uptake of fluorescently-labeled molecules. This rapid and technically simple approach is highly versatile and can readily be applied to characterize all major CPP properties that normally require multiple assays, including amount taken up by cells (in moles/cell), uptake efficiency, internalization pathways, intracellular distribution, intracellular degradation and toxicity threshold. The FACS-FCS approach provides a means for quantifying any intracellular biochemical entity, whether expressed in the cell or introduced exogenously and transported across the plasma membrane. (C) 2016 The Authors. Published by Elsevier B.V.
引用
收藏
页码:1499 / 1506
页数:8
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